- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04140656
The Effects of Plantar Sensory Based Physiotherapy Interventions on Balance and Fallings of Nursing Home Elderly
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study is planned to be conducted between the years of 2019-January-2020 for elderly people over 70 years old who live in Küçük Çamlıca Fahrettin Kerim Gökay Nursing Home. The study was planned as a randomized controlled clinical trial; By simple randomization method, cases will be divided into two groups. There are 47 elderly people over 70 years old in the nursing home to be studied. The sample size was planned to be 16 for each group.Group 1 (n:16), group 2 (n:17). 40 minutes / 3 days per week / 8 weeks long program will be applied to both groups. Four weeks after the first measurement, the second measurement was performed. Thus, pilot study was made. After the second measurement, rehabilitation program was started in both groups.After the 8-week program is finished, the third measurements will be made. After the third measurements, the fourth measurement will be done 4 weeks later for late results.The measurements are as follows.
Primary results: electronic pedobarography device for static and dynamic base pressure changes. Biodex balance test for measuring fall risk and static stability. For secondary results; 30 second Chair stand test, Berg balance scale, Semmes weinstein monofilament test.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey
- İstanbul Medipol University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Voluntariness
- 70 years and older
- Cognitive functions are sufficient for communication (MM score 22 and above)
- 20 meters independent walk
- The soles of the soles are at least at the reduced protective sensory level
Exclusion Criteria:
- Severe visual loss
- A history of mental retardation or schizophrenia
- Person has any problems to prevent walking
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Plantar sensitive exercise group
Plantar sensitive exercises:
|
Plantar sensitive exercises: 40 minutes / 3 days per week / 8 weeks Warm up exercise (5 minute) Walking on different 4 different textured floors and hot floor (15 minute) Trying to recognize small objects with the soles of the feet (5min) Seated work with barbed ball and balance pad (5min) Massage to the sole of the foot with different textured fabrics (5min) Cooling exercise (5 min) |
|
Active Comparator: Textured insole group
|
Textured insole group. Plantar sensitive exercises with insole 40 minutes / 3 days per week / 8 weeks (all exercises will be done with insoles) Warm up exercise (5 minute) Walking on flat ground (15 minute) Exercise with roller under the sole of the foot (5 minute) Seated work with barbed balance pad (5 min) Dorsi flexion and plantar flexion and hip flexion exercises (5min). Cooling exercise (5 min) |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pedobarographic investigation
Time Frame: day 0 (before intervention)
|
By means of pressure sensors in force platforms, foot pressure is detected and transferred to computer environment.
Static and dynamic measurement is also possible.
Plantar pressure can be measured as total and divided areas and it will be combined to report g/cm2.
Plantar contact area can be measured as total and divided areas and it will be combined to report cm2.
|
day 0 (before intervention)
|
|
Pedobarographic investigation
Time Frame: 4 weeks
|
By means of pressure sensors in force platforms, foot pressure is detected and transferred to computer environment.
Static and dynamic measurement is also possible.
Plantar pressure can be measured as total and divided areas and it will be combined to report g/cm2.
Plantar contact area can be measured as total and divided areas and it will be combined to report cm2.
|
4 weeks
|
|
Pedobarographic investigation
Time Frame: 12 weeks
|
By means of pressure sensors in force platforms, foot pressure is detected and transferred to computer environment.
Static and dynamic measurement is also possible.
Plantar pressure can be measured as total and divided areas and it will be combined to report g/cm2.
Plantar contact area can be measured as total and divided areas and it will be combined to report cm2.
|
12 weeks
|
|
Pedobarographic investigation
Time Frame: 16 weeks
|
By means of pressure sensors in force platforms, foot pressure is detected and transferred to computer environment.
Static and dynamic measurement is also possible.
Plantar pressure can be measured as total and divided areas and it will be combined to report g/cm2.
Plantar contact area can be measured as total and divided areas and it will be combined to report cm2.
|
16 weeks
|
|
Biodex Balance System
Time Frame: day 0 (before intervention)
|
It is a multi-axis device which objectively measures the balance of the person in static state or under dynamic stress and records the measurement results.
The Biodex Balance System permits a 20 ° inclination of the foot platform in all directions.
Thus, it provides maximum stimulation of the mechanical sensors in the ankle.
Biodex Balance System measurements are calculated in degrees for each direction It can be done by creating a dynamic environment for the measurement of fall risk on the same platform .
|
day 0 (before intervention)
|
|
Biodex Balance System
Time Frame: 4 weeks
|
It is a multi-axis device which objectively measures the balance of the person in static state or under dynamic stress and records the measurement results.
The Biodex Balance System permits a 20 ° inclination of the foot platform in all directions.
Thus, it provides maximum stimulation of the mechanical sensors in the ankle.
Biodex Balance System measurements are calculated in degrees for each direction It can be done by creating a dynamic environment for the measurement of fall risk on the same platform .
|
4 weeks
|
|
Biodex Balance System
Time Frame: 12 weeks
|
It is a multi-axis device which objectively measures the balance of the person in static state or under dynamic stress and records the measurement results.
The Biodex Balance System permits a 20 ° inclination of the foot platform in all directions.
Thus, it provides maximum stimulation of the mechanical sensors in the ankle.
Biodex Balance System measurements are calculated in degrees for each direction It can be done by creating a dynamic environment for the measurement of fall risk on the same platform .
|
12 weeks
|
|
Biodex Balance System
Time Frame: 16 weeks
|
It is a multi-axis device which objectively measures the balance of the person in static state or under dynamic stress and records the measurement results.
The Biodex Balance System permits a 20 ° inclination of the foot platform in all directions.
Thus, it provides maximum stimulation of the mechanical sensors in the ankle.
Biodex Balance System measurements are calculated in degrees for each direction It can be done by creating a dynamic environment for the measurement of fall risk on the same platform .
|
16 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Berg Balance Scala
Time Frame: day 0 (before intervention)
|
It is a 14-item clinical scale evaluating static and dynamic equilibrium abilities, each section rated from 0 (poor) to 4 (best).
The highest score is 56.
A score of less than 45 is an indicator of addiction in daily life.
Evaluates the level of dependence and / or independence during positions such as standing up from sitting, standing with feet adjacent, standing in tandem position, staying in balance on one leg and ability to change position.
The highest scores indicate the best balance score.
|
day 0 (before intervention)
|
|
Berg Balance Scala
Time Frame: 4 weeks
|
It is a 14-item clinical scale evaluating static and dynamic equilibrium abilities, each section rated from 0 (poor) to 4 (best).
The highest score is 56.
A score of less than 45 is an indicator of addiction in daily life.
Evaluates the level of dependence and / or independence during positions such as standing up from sitting, standing with feet adjacent, standing in tandem position, staying in balance on one leg and ability to change position.
The highest scores indicate the best balance score
|
4 weeks
|
|
Berg Balance Scala
Time Frame: 12 weeks
|
It is a 14-item clinical scale evaluating static and dynamic equilibrium abilities, each section rated from 0 (poor) to 4 (best).
The highest score is 56.
A score of less than 45 is an indicator of addiction in daily life.
Evaluates the level of dependence and / or independence during positions such as standing up from sitting, standing with feet adjacent, standing in tandem position, staying in balance on one leg and ability to change position.
The highest scores indicate the best balance score
|
12 weeks
|
|
Berg Balance
Time Frame: 16 weeks
|
It is a 14-item clinical scale evaluating static and dynamic equilibrium abilities, each section rated from 0 (poor) to 4 (best).
The highest score is 56.
A score of less than 45 is an indicator of addiction in daily life.
Evaluates the level of dependence and / or independence during positions such as standing up from sitting, standing with feet adjacent, standing in tandem position, staying in balance on one leg and ability to change position.
The highest scores indicate the best balance score
|
16 weeks
|
|
30 Second Chair Stand Test
Time Frame: day 0 (before intervention)
|
A test that assesses the person's sit-up activity, lower extremity strength and dynamic balance.
Number of sitting and getting up in 30 seconds is noted.
|
day 0 (before intervention)
|
|
30 Second Chair Stand Test
Time Frame: 4 weeks
|
A test that assesses the person's sit-up activity, lower extremity strength and dynamic balance.
Number of sitting and getting up in 30 seconds is noted.
|
4 weeks
|
|
30 Second Chair Stand Test
Time Frame: 12 weeks
|
A test that assesses the person's sit-up activity, lower extremity strength and dynamic balance.
Number of sitting and getting up in 30 seconds is noted.
|
12 weeks
|
|
30 Second Chair Stand Test
Time Frame: 16 weeks
|
A test that assesses the person's sit-up activity, lower extremity strength and dynamic balance.
Number of sitting and getting up in 30 seconds is noted.
|
16 weeks
|
|
Semmes Weinstein Monofilament Test
Time Frame: day 0 (before intervention)
|
Consists of 6 different diameter and equal length monofilments.
The test of the sense of touch by questioning whether the person feels the monofilament touches while their eyes are closed.
|
day 0 (before intervention)
|
|
Semmes Weinstein Monofilament Test
Time Frame: 4 weeks
|
Consists of 6 different diameter and equal length monofilments.
The test of the sense of touch by questioning whether the person feels the monofilament touches while their eyes are closed.
|
4 weeks
|
|
Semmes Weinstein Monofilament Test
Time Frame: 12 weeks
|
Consists of 6 different diameter and equal length monofilments.
The test of the sense of touch by questioning whether the person feels the monofilament touches while their eyes are closed.
|
12 weeks
|
|
Semmes Weinstein Monofilament Test
Time Frame: 16 weeks
|
Consists of 6 different diameter and equal length monofilments.
The test of the sense of touch by questioning whether the person feels the monofilament touches while their eyes are closed.
|
16 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Candan ALGUN, Prof, Medipol University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 10840098-604.01.01-E52392
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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